Á lódáil...
Familial vestibulocerebellar disorder maps to chromosome 13q31-q33: a new nystagmus locus
Design: Observational and experimental study. Methods: We carried out a phenotypic study of a unique four generation family with nystagmus. We performed genetic linkage studies including a genome wide search. Results: Affected family members developed vestibulocerebellar type nystagmus in the first...
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| Main Authors: | , , , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
BMJ Group
2003
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735258/ https://ncbi.nlm.nih.gov/pubmed/12525540 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.40.1.37 |
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